List of variants reported as uncertain significance for congenital secretory chloride diarrhea 1 by Fulgent Genetics, Fulgent Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000111.3(SLC26A3):c.455G>A (p.Arg152His)	rs763721296	0.00003
NM_000111.3(SLC26A3):c.1136G>C (p.Gly379Ala)	rs386833446	0.00001
NM_000111.3(SLC26A3):c.1843G>A (p.Val615Ile)
NM_000111.3(SLC26A3):c.431C>T (p.Ala144Val)

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